Transferring the blues

Autor: Lucinda V. Scott, Paul Ross, Timothy G. Dinan, Catherine Stanton, Ciaran O' Brien, Sahar El Aidy, Alan E. Hoban, Elaine Patterson, John F. Cryan, Patrick Fitzgerald, Gerard Clarke, S. Beers, John R. Kelly, Yuliya E. Borre, Jennifer Deane, Gerard M. Moloney, Paul J. Kennedy, Karen A. Scott
Přispěvatelé: Host-Microbe Interactions
Jazyk: angličtina
Rok vydání: 2016
Předmět:
Lipopolysaccharides
Male
0301 basic medicine
Hydrocortisone
Gut flora
Rats
Sprague-Dawley

Feces
chemistry.chemical_compound
0302 clinical medicine
fluids and secretions
RNA
Ribosomal
16S

Kynurenine
Depression (differential diagnoses)
biology
Depression
Middle Aged
Pathophysiology
Psychiatry and Mental health
C-Reactive Protein
Cytokines
Female
medicine.symptom
Lipopolysaccharide binding protein
Adult
medicine.medical_specialty
Gut–brain axis
Inflammation
digestive system
Food Preferences
03 medical and health sciences
Internal medicine
medicine
Animals
Humans
Maze Learning
Biological Psychiatry
Aged
Anhedonia
biology.organism_classification
Gastrointestinal Microbiome
Rats
Gastrointestinal Tract
Disease Models
Animal

stomatognathic diseases
030104 developmental biology
Endocrinology
chemistry
Case-Control Studies
Immunology
biology.protein
Corticosterone
030217 neurology & neurosurgery
Zdroj: Journal of Psychiatric Research, 82, 109-118. PERGAMON-ELSEVIER SCIENCE LTD
ISSN: 0022-3956
Popis: The gut microbiota interacts with the host via neuroimmune, neuroendocrine and neural pathways. These pathways are components of the brain-gut-microbiota axis and preclinical evidence suggests that the microbiota can recruit this bidirectional communication system to modulate brain development, function and behaviour. The pathophysiology of depression involves neuroimmune-neuroendocrine dysregulation. However, the extent to which changes in gut microbiota composition and function mediate the dysregulation of these pathways is unknown. Thirty four patients with major depression and 33 matched healthy controls were recruited. Cytokines, CRP, Salivary Cortisol and plasma Lipopolysaccharide binding protein were determined by ELISA. Plasma tryptophan and kynurenine were determined by HPLC. Fecal samples were collected for 16s rRNA sequencing. A Fecal Microbiota transplantation was prepared from a sub group of depressed patients and controls and transferred by oral gavage to a microbiota-deficient rat model. We demonstrate that depression is associated with decreased gut microbiota richness and diversity. Fecal microbiota transplantation from depressed patients to microbiota-depleted rats can induce behavioural and physiological features characteristic of depression in the recipient animals, including anhedonia and anxiety-like behaviours, as well as alterations in tryptophan metabolism. This suggests that the gut microbiota may play a causal role in the development of features of depression and may provide a tractable target in the treatment and prevention of this disorder.
Databáze: OpenAIRE